17878-23-8

Basic information

• Product Name: 3,5-DIBROMO-1-TRIMETHYLSILYLBENZENE
• Synonyms: 3,5-DIBROMO-1-TRIMETHYLSILYLBENZENE;(3,5-DIBROMOPHENYL)TRIMETHYLSILANE
• CAS NO: 17878-23-8
• Molecular Formula: C₉H₁₂Br₂Si
• Molecular Weight: 308.09
• Product Categories: Building Blocks for Dendrimers;Functional Materials;Si (Classes of Silicon Compounds);Si-(C)4 Compounds
• Mol File: 17878-23-8.mol

Chemical Properties

• Melting Point: 40 °C
• Boiling Point: 280.1°C at 760 mmHg
• Flash Point: 176.9°C
• Appearance: /
• Density: 1.53g/cm³
• Vapor Pressure: 0.00656mmHg at 25°C
• Refractive Index: 1.558
• CAS DataBase Reference: 3,5-DIBROMO-1-TRIMETHYLSILYLBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-DIBROMO-1-TRIMETHYLSILYLBENZENE(17878-23-8)
• EPA Substance Registry System: 3,5-DIBROMO-1-TRIMETHYLSILYLBENZENE(17878-23-8)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 17878-23-8(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
3,5-DIBROMO-1-TRIMETHYLSILYLBENZENE is utilized as a key intermediate for the synthesis of pharmaceutical compounds. Its reactivity and functional groups facilitate the creation of new drug molecules with enhanced therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 3,5-DIBROMO-1-TRIMETHYLSILYLBENZENE is employed as a precursor in the development of novel agrochemicals. Its chemical versatility aids in the production of more effective and targeted pesticides and other agricultural chemicals.
Used in Materials Science:
3,5-DIBROMO-1-TRIMETHYLSILYLBENZENE is used as a building block in the synthesis of advanced materials with specific properties. Its role in materials science is crucial for the development of new polymers, composites, and other materials with tailored characteristics for various applications.
Used in Organic Synthesis:
3,5-DIBROMO-1-TRIMETHYLSILYLBENZENE is leveraged as a versatile reactant in organic synthesis. Its ability to participate in cross-coupling and nucleophilic aromatic substitution reactions makes it an indispensable tool for the creation of complex organic molecules.
Used in Molecular Modification:
3,5-DIBROMO-1-TRIMETHYLSILYLBENZENE is also used for the modification of existing organic molecules to enhance their properties. The presence of bromine and the trimethylsilyl group allows for targeted functionalization and property enhancement in various organic systems.

InChI:InChI=1/C9H12Br2Si/c1-12(2,3)9-5-7(10)4-8(11)6-9/h4-6H,1-3H3

Upstream product

• 75-76-3 tetramethylsilane 
• 626-39-1 1,3,5-trisbromobenzene 
• 75-77-4 chloro-trimethyl-silane 
• 19752-57-9 1,3-dibromo-5-iodobenzene 

Downstream Products

• 943024-31-5 C₃₅H₃₄O₂Si 
• 750573-24-1 9,9’-(5-bromo-1,3-phenylene)bis(9H-carbazole) 
• 950603-55-1 3-bromo-5-(trimethylsilyl)phenylboronic acid 
• 87581-78-0 {3-bromo-5-(trimethylgermyl)phenyl}trimethylsilane 
• 87590-12-3 (3-bromo-5-(trimethylstannyl)phenyl)trimethylsilane 
• 128388-56-7 C₆H₃(C₆H₅(C₆H₄)2)2BO₂H₂ 
• 128388-55-6 5-(trimethylsilyl)-1,3-bis(1',3'-diphenylphenyl)benzene 
• 453538-48-2 trimethyl(4-{3-[3,5,3'',5''-tetrakis(3-benzyloxypropyl)[1,1':3',1'']terphenyl-5'-yl]propyl}phenyl)silane 
• 453538-58-4 2-(4-{3-[4,4''-bis(3-benzyloxypropyl)[1,1';3',1'']terphenyl-5'-yl]propyl}phenyl)-4,4,5,5-tetramethyl[1,3,2]dioxaborolane 
• 453538-57-3 4-{3-[4,4''-bis(3-benzyloxypropyl)[1,1;3',1'']terphenyl-5'-yl]propyl}phenylboronic acid 
• 453538-55-1 (4-{3-[4,4''-bis(3-benzyloxypropyl)[1,1';3',1'']terphenyl-5'-yl]propyl}phenyl)trimethylsilane 
• 453538-56-2 4,4''-bis(3-benzyloxypropyl)-5'-[3-(4-iodophenyl)propyl][1,1';3;1'']terphenyl 
• 453538-43-7 {4-[3-(3,5-dibromophenyl)propyl]phenyl}trimethylsilane 
• 1027302-33-5 C₅₆H₇₈Br₂O₅Si 

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